Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease. - Wikidata - wikimedia - TriplyDB

Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease.

Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease.

http://www.wikidata.org/entity/Q43617306

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Common polymorphisms influencing serum uric acid levels contribute to susceptibility to gout, but not to coronary artery disease RNAi-based functional profiling of loci from blood lipid genome-wide association studies identifies genes with cholesterol-regulatory function The impact of genome-wide association studies on the pathophysiology and therapy of cardiovascular disease Genetic epidemiology of coronary artery disease: an Asian Indian perspective Genetic prediction of common diseases. Still no help for the clinical diabetologist!Genetics of coronary artery disease Human Genetics and the Causal Role of Lipoprotein(a) for Various Diseases Lipoprotein(a) and risk of myocardial infarction--genetic epidemiologic evidence of causality Large-scale gene-centric analysis identifies novel variants for coronary artery disease Caution in interpreting results from imputation analysis when linkage disequilibrium extends over a large distance: a case study on venous thrombosis A latent variable partial least squares path modeling approach to regional association and polygenic effect with applications to a human obesity study Large scale association analysis identifies three susceptibility loci for coronary artery disease Genetics of venous thrombosis: insights from a new genome wide association study Systematic haplotype analysis resolves a complex plasma plant sterol locus on the Micronesian Island of Kosrae Genetics and beyond--the transcriptome of human monocytes and disease susceptibility Genome-wide association study of coronary artery disease in the Japanese A genome-wide association study of a coronary artery disease risk variant Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.Macrophages in the pathogenesis of atherosclerosis Lipoprotein (a) as a cause of cardiovascular disease: insights from epidemiology, genetics, and biology Detailed analysis of association between common single nucleotide polymorphisms and subclinical atherosclerosis: The Multi-ethnic Study of Atherosclerosis.Common genetic variants and subclinical atherosclerosis: The Multi-Ethnic Study of Atherosclerosis (MESA).Characterization of Ath29, a major mouse atherosclerosis susceptibility locus, and identification of Rcn2 as a novel regulator of cytokine expression Genetic variation in LPAL2, LPA, and PLG predicts plasma lipoprotein(a) level and carotid artery disease risk.Accurate estimation of haplotype frequency from pooled sequencing data and cost-effective identification of rare haplotype carriers by overlapping pool sequencing.Ehapp2: Estimate haplotype frequencies from pooled sequencing data with prior database information.A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.Expression of organic cation transporters OCT1 (SLC22A1) and OCT3 (SLC22A3) is affected by genetic factors and cholestasis in human liver.The interleukin-1 cluster, dyslipidaemia and risk of myocardial infarction Telomere biology in healthy aging and disease.Effect of diet-induced weight loss on lipoprotein(a) levels in obese individuals with and without type 2 diabetes Towards a molecular systems model of coronary artery disease Implications of genetic polymorphisms in inflammation-induced atherosclerosis Genome-Wide Linkage Analysis of Large Multiple Multigenerational Families Identifies Novel Genetic Loci for Coronary Artery Disease.LPA rs10455872 polymorphism is associated with coronary lesions in Brazilian patients submitted to coronary angiography Genome-wide association analysis of incident coronary heart disease (CHD) in African Americans: a short report Recent methods for polygenic analysis of genome-wide data implicate an important effect of common variants on cardiovascular disease risk.Lipoprotein(a) levels and long-term cardiovascular risk in the contemporary era of statin therapy.The role of endoplasmic reticulum stress in the progression of atherosclerosis.Genetic profiling using genome-wide significant coronary artery disease risk variants does not improve the prediction of subclinical atherosclerosis: the Cardiovascular Risk in Young Finns Study, the Bogalusa Heart Study and the Health 2000 Survey--

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Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease.

http://www.wikidata.org/entity/Q43617306

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Genome-wide haplotype associat ...... s for coronary artery disease.

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Genome-wide haplotype associat ...... s for coronary artery disease.

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Genome-wide haplotype associat ...... s for coronary artery disease.

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Nature Genetics

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Alexandru Munteanu

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Alun Evans

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Anika Grosshennig

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Anthony J Balmforth

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Arne Schäfer

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Ben J Wright

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Cardiogenics Consortium

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Christian Hengstenberg

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Claire Perret

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P2860

Genomewide association analysis of coronary artery disease

Haplotypic analysis of Wellcome Trust Case Control Consortium data.

Apolipoprotein(a) gene accounts for greater than 90% of the variation in plasma lipoprotein(a) concentrations

PopGen: population-based recruitment of patients and controls for the analysis of complex genotype-phenotype relationships.

Building an infrastructure for scientific Grid computing: status and goals of the EGEE project.

Distinct Heritable Patterns of Angiographic Coronary Artery Disease in Families With Myocardial Infarction

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283-285

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10.1038/NG.314

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3

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41

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Thomas Meitinger

Heribert Schunkert

Jeanette Erdmann

Andreas Ziegler

Christa Meisinger

Pim van der Harst

Patrick Linsel-Nitschke

Alistair Scott Hall

Willem H Ouwehand

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2009-02-08T00:00:00Z

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